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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1483220생성일: 2026년 10월 26일

Acetaldehyde → 6-Ethyl-2-(ethylamino)-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-3-carboxamide

https://huagongshe.com/reaction/1483220

반응식

참여 물질

역할이름HCID투입량
반응물AcetaldehydeHCID 177—
반응물Sulfuric acid magnesium salt (1:1)HCID 24083—
반응물2-Amino-6-ethyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-3-carboxamideHCID 614439—
반응물Sodium cyanoborohydrideHCID 5003444—
촉매Acetic AcidHCID 176—
용매MethanolHCID 887—
용매TetrahydrofuranHCID 8028—
생성물6-Ethyl-2-(ethylamino)-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-3-carboxamideHCID 6805921680.4%

반응 단계

To a stirred mixture of compound F4 (200 mg, 0.888 mmol), acetaldehyde (5 M in tetrahydrofuran, 0.360 mL, 1.80 mmol), acetic acid (two drops), anhydrous magnesium sulfate (200 mg) in anhydrous methanol (6 mL) and anhydrous tetrahydrofuran (3 mL) was added sodium cyanoborohydride (167 mg, 2.66 mmol) at room temperature under nitrogen. The reaction mixture was stirred for 23 h and then filtered. The filtrate was concentrated. The resulting residue was purified by flash column chromatography on silica gel eluting with 10% to 20% methanol/methylene chloride to afford compound R1 as a colourless syrup (181 mg, 80%): MS (M+H) 254.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09416141B2
출처 데이터셋uspto-grants-2016_08
ORD IDord-936824ed268141a19c4edc04c2fab9e6
출처 메모uspto-grants-2016_08